Synthesis and Application of Bioactive N‐Functionalized Aziridines
This review discusses modern synthetic methods for the preparation of aziridine‐containing small molecules, including biocatalytic, electrocatalytic, and photocatalytic strategies. We highlight the compatibility of various synthetic methods with control of the exocyclic N‐substituent.
Hao Tan +4 more
wiley +1 more source
Amine-Promoted Alkene Aziridination
Aziridines, the smallest saturated aza-heterocycle, are not only prevalent in several natural products, but also represent a versatile synthetic tool for the chemist via exploitation of the strained ring system. Research described in this thesis concerns
Pullin, Robert David Charles +1 more
core +1 more source
Dentro de la megafitodiversidad del Perú, se enmarcan muchas especies de los géneros Cinchona, Ladenbergia y Remijia; conocidas indistintamente por los pobladores de las Comunidades andino-amazónicas como “árboles de la quina”, “quina” o “cascarillas” y ...
Segundo E. López Medina +5 more
doaj
Professor Dragendorffi teadustegevuse jäljed Tartu Ülikooli ajaloo muuseumi kogudes [PDF]
Evidence of Dragendorff’s scientific work inThe University of Tartu History MuseumCollectionsJ. G. N. Dragendorff (20.04.1836 – 26.03.1898) was a Professor of Pharmacy at the University of Tartu from 1864 to 1894.
Sisask, Sirje
core +3 more sources
Current status of herbal and their future perspectives [PDF]
Traditional medicine is the synthesis of therapeutic experience of generations of practicing physicians of indigenous systems of medicine. Throughout the history of mankind, many infectious diseases have been treated with herbals.
Ponnampalam Gopalakrishnakone +1 more
core +1 more source
Chiral separation by enantioselective liquid–liquid extraction [PDF]
The literature on enantioselective liquid–liquid extraction (ELLE) spans more than half a century of research. Nonetheless, a comprehensive overview has not appeared during the past few decades.
Feringa, Ben L., +5 more
core +3 more sources
Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
Decarboxylative aldol reaction of aliphatic carboxylic acids is a useful method for C−C bond formation because carboxylic acids are an easily available class of compounds. In this study, we found that the decarboxylative aldol reaction of tertiary &
Ryouta Kawanishi +3 more
doaj +1 more source
Quinidine-Catalysed Enantioselective Synthesis of 6- and 4-Trifluoromethyl-Substituted Dihydropyrans [PDF]
The authors thank the Royal Society for a University Research Fellowship (ADS) and the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013), ERC Grant Agreement No. 279850 (KK), the authors also thank the EPSRC
Ashtekar +48 more
core +1 more source
Asymmetric α‐Chlorination of β‐Keto Esters Using Hypervalent Iodine‐Based Cl‐Transfer Reagents in Combination with Cinchona Alkaloid Catalysts [PDF]
Lotte Stockhammer +3 more
openalex +1 more source
Naturally based ionic liquids with indole-3-acetate anions and cations derived from cinchona alkaloids. [PDF]
Rzemieniecki T, Kleiber T, Pernak J.
europepmc +1 more source

